BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

380 related articles for article (PubMed ID: 26475045)

  • 1. Genome-wide significant association with seven novel multiple sclerosis risk loci.
    Lill CM; Luessi F; Alcina A; Sokolova EA; Ugidos N; de la Hera B; Guillot-Noël L; Malhotra S; Reinthaler E; Schjeide BM; Mescheriakova JY; Mashychev A; Wohlers I; Akkad DA; Aktas O; Alloza I; Antigüedad A; Arroyo R; Astobiza I; Blaschke P; Boyko AN; Buttmann M; Chan A; Dörner T; Epplen JT; Favorova OO; Fedetz M; Fernández O; García-Martínez A; Gerdes LA; Graetz C; Hartung HP; Hoffjan S; Izquierdo G; Korobko DS; Kroner A; Kubisch C; Kümpfel T; Leyva L; Lohse P; Malkova NA; Montalban X; Popova EV; Rieckmann P; Rozhdestvenskii AS; Schmied C; Smagina IV; Tsareva EY; Winkelmann A; Zettl UK; Binder H; Cournu-Rebeix I; Hintzen R; Zimprich A; Comabella M; Fontaine B; Urcelay E; Vandenbroeck K; Filipenko M; Matesanz F; Zipp F; Bertram L
    J Med Genet; 2015 Dec; 52(12):848-55. PubMed ID: 26475045
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.
    Hoppenbrouwers IA; Aulchenko YS; Janssens AC; Ramagopalan SV; Broer L; Kayser M; Ebers GC; Oostra BA; van Duijn CM; Hintzen RQ
    J Hum Genet; 2009 Nov; 54(11):676-80. PubMed ID: 19834503
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis.
    Matesanz F; Potenciano V; Fedetz M; Ramos-Mozo P; Abad-Grau Mdel M; Karaky M; Barrionuevo C; Izquierdo G; Ruiz-Peña JL; García-Sánchez MI; Lucas M; Fernández Ó; Leyva L; Otaegui D; Muñoz-Culla M; Olascoaga J; Vandenbroeck K; Alloza I; Astobiza I; Antigüedad A; Villar LM; Álvarez-Cermeño JC; Malhotra S; Comabella M; Montalban X; Saiz A; Blanco Y; Arroyo R; Varadé J; Urcelay E; Alcina A
    Hum Mol Genet; 2015 Oct; 24(19):5619-27. PubMed ID: 26152201
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
    Patsopoulos NA; ; ; ; ; ; Esposito F; Reischl J; Lehr S; Bauer D; Heubach J; Sandbrink R; Pohl C; Edan G; Kappos L; Miller D; Montalbán J; Polman CH; Freedman MS; Hartung HP; Arnason BG; Comi G; Cook S; Filippi M; Goodin DS; Jeffery D; O'Connor P; Ebers GC; Langdon D; Reder AT; Traboulsee A; Zipp F; Schimrigk S; Hillert J; Bahlo M; Booth DR; Broadley S; Brown MA; Browning BL; Browning SR; Butzkueven H; Carroll WM; Chapman C; Foote SJ; Griffiths L; Kermode AG; Kilpatrick TJ; Lechner-Scott J; Marriott M; Mason D; Moscato P; Heard RN; Pender MP; Perreau VM; Perera D; Rubio JP; Scott RJ; Slee M; Stankovich J; Stewart GJ; Taylor BV; Tubridy N; Willoughby E; Wiley J; Matthews P; Boneschi FM; Compston A; Haines J; Hauser SL; McCauley J; Ivinson A; Oksenberg JR; Pericak-Vance M; Sawcer SJ; De Jager PL; Hafler DA; de Bakker PI
    Ann Neurol; 2011 Dec; 70(6):897-912. PubMed ID: 22190364
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease.
    Al Jumah M; Al Balwi M; Hussein M; Kojan S; Al Khathaami A; Al Fawaz M; Al Muzaini B; Jawhary A; Al Abdulkareem I
    Mult Scler; 2012 Oct; 18(10):1395-400. PubMed ID: 22492128
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Risk alleles for multiple sclerosis in multiplex families.
    D'Netto MJ; Ward H; Morrison KM; Ramagopalan SV; Dyment DA; DeLuca GC; Handunnetthi L; Sadovnick AD; Ebers GC
    Neurology; 2009 Jun; 72(23):1984-8. PubMed ID: 19506219
    [TBL] [Abstract][Full Text] [Related]  

  • 7. EVI5 is a risk gene for multiple sclerosis.
    Hoppenbrouwers IA; Aulchenko YS; Ebers GC; Ramagopalan SV; Oostra BA; van Duijn CM; Hintzen RQ
    Genes Immun; 2008 Jun; 9(4):334-7. PubMed ID: 18401352
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome-wide association study and meta-analysis in multiple populations identifies new loci for peanut allergy and establishes C11orf30/EMSY as a genetic risk factor for food allergy.
    Asai Y; Eslami A; van Ginkel CD; Akhabir L; Wan M; Ellis G; Ben-Shoshan M; Martino D; Ferreira MA; Allen K; Mazer B; de Groot H; de Jong NW; Gerth van Wijk RN; Dubois AEJ; Chin R; Cheuk S; Hoffman J; Jorgensen E; Witte JS; Melles RB; Hong X; Wang X; Hui J; Musk AWB; Hunter M; James AL; Koppelman GH; Sandford AJ; Clarke AE; Daley D
    J Allergy Clin Immunol; 2018 Mar; 141(3):991-1001. PubMed ID: 29030101
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus.
    Perera D; Stankovich J; Butzkueven H; Taylor BV; Foote SJ; Kilpatrick TJ; Rubio JP
    J Neuroimmunol; 2009 Jun; 211(1-2):105-9. PubMed ID: 19375175
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association between CD24-P226-C/T polymorphism and multiple sclerosis: a meta-analysis.
    Jiang L; Bai X; Wang Y; Wei M
    Immunol Invest; 2015; 44(4):321-30. PubMed ID: 25942344
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association to the Glypican-5 gene in multiple sclerosis.
    Lorentzen AR; Melum E; Ellinghaus E; Smestad C; Mero IL; Aarseth JH; Myhr KM; Celius EG; Lie BA; Karlsen TH; Franke A; Harbo HF
    J Neuroimmunol; 2010 Sep; 226(1-2):194-7. PubMed ID: 20692050
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain.
    Swaminathan B; Matesanz F; Cavanillas ML; Alloza I; Otaegui D; Olascoaga J; Cénit MC; de las Heras V; Barcina MG; Arroyo R; Alcina A; Fernandez O; Antigüedad A; Urcelay E; Vandenbroeck K
    J Neuroimmunol; 2010 Jun; 223(1-2):100-3. PubMed ID: 20430450
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians.
    Rubio JP; Stankovich J; Field J; Tubridy N; Marriott M; Chapman C; Bahlo M; Perera D; Johnson LJ; Tait BD; Varney MD; Speed TP; Taylor BV; Foote SJ; Butzkueven H; Kilpatrick TJ
    Genes Immun; 2008 Oct; 9(7):624-30. PubMed ID: 18650830
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.
    Julià A; Domènech E; Ricart E; Tortosa R; García-Sánchez V; Gisbert JP; Nos Mateu P; Gutiérrez A; Gomollón F; Mendoza JL; Garcia-Planella E; Barreiro-de Acosta M; Muñoz F; Vera M; Saro C; Esteve M; Andreu M; Alonso A; López-Lasanta M; Codó L; Gelpí JL; García-Montero AC; Bertranpetit J; Absher D; Panés J; Marsal S
    Gut; 2013 Oct; 62(10):1440-5. PubMed ID: 22936669
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of the IL28RA locus as genetic risk factor for multiple sclerosis.
    Lopez de Lapuente A; Alloza I; Goertsches R; Zettl UK; Urcelay E; Arroyo R; Comabella M; Montalban X; Antigüedad A; Vandenbroeck K
    J Neuroimmunol; 2012 Apr; 245(1-2):98-101. PubMed ID: 22386267
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population.
    Ludwig KU; Wahle P; Reutter H; Paredes-Zenteno M; Muñoz-Jimenez SG; Ortiz-Lopez R; Böhmer AC; Tessmann P; Nowak S; Nöthen MM; Knapp M; Rojas-Martinez A; Mangold E
    Birth Defects Res A Clin Mol Teratol; 2014 Jan; 100(1):43-7. PubMed ID: 24382704
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [New gene map for multiple sclerosis].
    Harbo HF; Lorentzen AR; Lie BA; Celius EG; Spurkland A
    Tidsskr Nor Laegeforen; 2011 Nov; 131(21):2126-30. PubMed ID: 22048209
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Risk genes associated with pediatric-onset MS but not with monophasic acquired CNS demyelination.
    van Pelt ED; Mescheriakova JY; Makhani N; Ketelslegers IA; Neuteboom RF; Kundu S; Broer L; Janssens C; Catsman-Berrevoets CE; van Duijn CM; Banwell B; Bar-Or A; Hintzen RQ
    Neurology; 2013 Dec; 81(23):1996-2001. PubMed ID: 24198294
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis.
    ; Lill CM; Schjeide BM; Graetz C; Ban M; Alcina A; Ortiz MA; Pérez J; Damotte V; Booth D; Lopez de Lapuente A; Broer L; Schilling M; Akkad DA; Aktas O; Alloza I; Antigüedad A; Arroyo R; Blaschke P; Buttmann M; Chan A; Compston A; Cournu-Rebeix I; Dörner T; Epplen JT; Fernández Ó; Gerdes LA; Guillot-Noël L; Hartung HP; Hoffjan S; Izquierdo G; Kemppinen A; Kroner A; Kubisch C; Kümpfel T; Li SC; Lindenberger U; Lohse P; Lubetzki C; Luessi F; Malhotra S; Mescheriakova J; Montalban X; Papeix C; Paredes LF; Rieckmann P; Steinhagen-Thiessen E; Winkelmann A; Zettl UK; Hintzen R; Vandenbroeck K; Stewart G; Fontaine B; Comabella M; Urcelay E; Matesanz F; Sawcer S; Bertram L; Zipp F
    Brain; 2013 Jun; 136(Pt 6):1778-82. PubMed ID: 23739915
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Protein-protein interaction analysis highlights additional loci of interest for multiple sclerosis.
    Ragnedda G; Disanto G; Giovannoni G; Ebers GC; Sotgiu S; Ramagopalan SV
    PLoS One; 2012; 7(10):e46730. PubMed ID: 23094030
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.